Home NDC 48951-3041 Cartilago Betula
Product NDC 48951-3041
11-digit product format 489513041
Labeler code 48951
Product ID 48951-3041_4575c616-cb28-3bb1-e063-6394a90adb91
Type HUMAN OTC DRUG
Nonproprietary name Cartilago Betula
Dosage form PELLET
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BETULA PUBESCENS LEAF; ACONITUM NAPELLUS; ARNICA MONTANA; BOS TAURUS CARTILAGE; TIN; GOLD; ONION; FORMICA RUFA
Active strength 5; 6; 6; 8; 8; 10; 17; 17 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Cartilago Betula
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BETULA PUBESCENS LEAF 5 [hp_X]/1 ACONITUM NAPELLUS 6 [hp_X]/1 ARNICA MONTANA 6 [hp_X]/1 BOS TAURUS CARTILAGE 8 [hp_X]/1 TIN 8 [hp_X]/1 GOLD 10 [hp_X]/1 ONION 17 [hp_X]/1 FORMICA RUFA 17 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-3041-2 Cartilago Betula 1350 in 1 BOTTLE, GLASS PELLET 1350 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-3041 CARTILAGO BETULA PELLET [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 1 package rows 20180601_99037dd6-b2c8-45d0-bb5f-670aed53ee46.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-3041-2 48951304102 1350 PELLET in 1 BOTTLE, GLASS (48951-3041-2) 1350 pellet 2009-09-01 0000-00-00 No No Current